Zhou Shuru, Chen Xin, Meng Xiaobin, Zhang Guoxiong, Wang Jie, Zhou Dongsheng, Guo Xuemin
1] Institute of Human Virology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, China [2] Key Laboratory of Tropical Disease Control at Sun Yat-Sen University, Ministry of Education, Guangzhou, China.
Meizhou People's Hospital, Meizhou, China.
Sci Rep. 2015 Mar 10;5:8976. doi: 10.1038/srep08976.
Acinetobacter pittii 44551 was recovered from a patient with gout combined with tuberculosis and was found to harbor the carbapenemase genes blaNDM-1 and blaOXA-58 on two different plasmids pNDM-44551 and pOXA58-44551, respectively. pNDM-44551 displayed high self-transferability across multiple bacterial species, while pOXA58-44551 was likely co-transferable with pNDM-44551 into A. baumannii receipts. pNDM-44551 was a close variant of the previously characterized pNDM-BJ01, and the blaNDM-1 gene cluster was arranged sequentially as orfA, ISAba14, aphA6, ISAba125, blaNDM-1, bleMBL, ΔtrpF, dsbC, tnpR, and zeta. pOXA58-44551 was a repAci9-containing plasmid, and blaOXA-58 was embedded in a 372F-ISAba3-like-blaOXA-58-ISAba3 structure. The mobile genetic platforms of blaNDM-1 and blaOXA-58 herein showed some differences from their previously characterized variants. The production of NDM-1 in strain 44551 contributed the majority to its high resistance to carbapenems, while the blaOXA-58 stayed silent most likely due to the lack of an upstream promoter to drive its transcription. Increased surveillance of Acinetobacter co-harboring blaNDM-1 (active) and blaOXA-58 (either active or silent) is urgently needed.
皮氏不动杆菌44551是从一名痛风合并结核病患者体内分离得到的,发现其在两个不同的质粒pNDM - 44551和pOXA58 - 44551上分别携带碳青霉烯酶基因blaNDM - 1和blaOXA - 58。pNDM - 44551在多种细菌物种间表现出高自我转移性,而pOXA58 - 44551可能与pNDM - 44551共同转移至鲍曼不动杆菌受体菌中。pNDM - 44551是先前鉴定的pNDM - BJ01的紧密变体,blaNDM - 1基因簇依次排列为orfA、ISAba14、aphA6、ISAba125、blaNDM - 1、bleMBL、ΔtrpF、dsbC、tnpR和zeta。pOXA58 - 44551是一个含repAci9的质粒,blaOXA - 58嵌入在一个372F - ISAba3样 - blaOXA - 58 - ISAba3结构中。本文中blaNDM - 1和blaOXA - 58的移动遗传平台与其先前鉴定的变体存在一些差异。菌株44551中NDM - 1的产生是其对碳青霉烯类药物高度耐药的主要原因,而blaOXA - 58很可能由于缺乏驱动其转录的上游启动子而保持沉默。迫切需要加强对同时携带blaNDM - 1(活性)和blaOXA - 58(活性或沉默)的不动杆菌的监测。